SURFACE X CUTIE PALS HAND SANITIZER CITRUS CRUSH- alcohol liquid

Surface x Cutie Pals Hand Sanitizer Citrus Crush by

Drug Labeling and Warnings

Surface x Cutie Pals Hand Sanitizer Citrus Crush by is a Otc medication manufactured, distributed, or labeled by I World LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Ethyl Alcohol 70% v/v

Purpose

Antibacterial

Uses

• For hand-washing to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable, keep away from fire and flames

When using this product

• test on a small area of skin before full use. keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask doctor if

• allergy, irritation or redness develops.
• Condition persists for more than 72 hours.

Keep out of reach of children.

• If product is swallowed, get medical help or contact a poison control center right away.

Directions

Spray hands with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Other information

Do not store above 105 °F May discolor some fabrics
Harmful to wood finishes and plastics

Inactive ingredients

WATER (AQUA), FRAGRANCE (PARFUM), LIMONENE, MENTHA VIRIDIS (SPEARMINT) LEAF OIL.

Questions or comments?

1-212- 244-5170  info@amora.beauty

Package Labeling:

INGREDIENTS AND APPEARANCE

SURFACE X CUTIE PALS HAND SANITIZER CITRUS CRUSH 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
SPEARMINT OIL (UNII: C3M81465G5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-010-00	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/02/2025

Labeler - I World LLC (830590126)

Registrant - I World LLC (830590126)